1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Basic information
- Product Name:
- 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
- Synonyms:
-
- 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
- 1, 1-ACCB(OME)
- Cyclobutanecarboxylic acid, 1-amino-, methyl ester (9CI)
- Cyclobutanecarboxylic acid, 1-aMino-, Methyl ester
- Methyl 1-aMinocyclobutanecarboxylate
- methyl 1-aminocyclobutane-1-carboxylate
- 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER USP/EP/BP
- Cyclobutanecarboxylicacid, 1-amino-, methyl ester, hydrochlo...
- CAS:
- 215597-35-6
- MF:
- C6H11NO2
- MW:
- 129.16
- Product Categories:
-
- AMINEPRIMARY
- AMINOACID
- pharmacetical
- Mol File:
- 215597-35-6.mol
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Chemical Properties
- Boiling point:
- 162.3±23.0 °C(Predicted)
- Density
- 1.127±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
- pka
- 7.71±0.20(Predicted)
- form
- Solid
- Appearance
- Colorless to light yellow Liquid
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Usage And Synthesis
Synthesis
67-56-1
120728-10-1
215597-35-6
Stage 1: Synthesis of methyl 1-aminocyclobutanecarboxylate Concentrated H2SO4 (10 ml) was slowly added to a methanol solution (30 ml) containing 1-(tert-butoxycarbonylamino)-cyclobutane-1-carboxylic acid (9.29 mmol, 1 eq.) at 0°C. The reaction mixture was refluxed at 0°C for 2 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in distilled water and the pH was adjusted to 8-9 with saturated sodium bicarbonate solution, followed by extraction with ethyl acetate (2 x 200 ml). The combined organic phases were washed sequentially with distilled water (2 x 150 ml) and saturated NaCl solution (2 x 50 ml) and dried with anhydrous sodium sulfate. Finally, the solvent was removed by concentration under reduced pressure to afford methyl 1-aminocyclobutanecarboxylate as a white solid in 75% yield.
References
[1] Patent: US2010/173889, 2010, A1. Location in patent: Page/Page column 34
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